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6-Bromo-2-pyridinecarbonitrile

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6-Bromo-2-pyridinecarbonitrile Basic information

Product Name:
6-Bromo-2-pyridinecarbonitrile
Synonyms:
  • 2-BROMO-6-CYANOPYRIDINE
  • 6-BROMO-PYRIDINE-2-CARBONITRILE
  • 6-BROMO-2-PYRIDINECARBONITRILE
  • 6-Bromo-2-cyanopyridine
  • 6-Bromopicolinonitrile
  • 6-Bromo-2-pyridinecarboni...
  • 6-Bromo-2-cyanopyridine, 6-Bromopicolinonitrile
  • 6-BroMo-2-pyridinecarbonitrile
CAS:
122918-25-6
MF:
C6H3BrN2
MW:
183.01
Product Categories:
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Pyridine series
  • Heterocyclic Compounds
  • Bases & Related Reagents
  • Pyridines
  • Heterocycles
  • Nucleotides
  • C6Heterocyclic Building Blocks
Mol File:
122918-25-6.mol
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6-Bromo-2-pyridinecarbonitrile Chemical Properties

Melting point:
100-104 °C
Boiling point:
269.7±20.0 °C(Predicted)
Density 
1.72±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
-4.76±0.10(Predicted)
form 
Low Melting Solid or Crystalline Powder
color 
White to off-white
InChIKey
HNEBPTAKURBYRM-UHFFFAOYSA-N
CAS DataBase Reference
122918-25-6(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
22-37/38-41-R41-R37/38-R22
Safety Statements 
26-39-S39-S26
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29333990
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6-Bromo-2-pyridinecarbonitrile Usage And Synthesis

Description

6-Bromo-2-pyridinecarbonitrile is a small molecule that can be used as a sensitizer for photovoltaic cells. It has been shown to have photocurrents in the visible region of the spectrum and strong luminescence properties. 6-Bromo-2-pyridinecarbonitrile is also an effective chromophore for use in solar cells and can be functionalized by means of pyrazolyl or triazolyl groups. This compound has been shown to bind to antibodies, which are proteins that are produced by the body's immune system to identify and neutralize foreign objects, including bacteria and viruses. The binding of 6-bromo-2-pyridinecarbonitrile with monoclonal antibodies provides a possible route for developing new biomolecules with antibacterial properties.

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